sodium bromate

Cc1sc(-c2ccc(C(F)(F)F)cc2)cc1CO
Reaction #9738
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)c1cc(-c2ccc(C(F)(F)F)cc2)oc1CBr
Reaction #9739
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(O)c1ccc(F)cc1
Reaction #42013
4-fluorobenzoic acid
Yield 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)c1ccc(F)cc1
Reaction #42014
4-fluorobenzoic acid
Yield 89.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)c1ccccc1
Reaction #42015
benzoic acid
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)c1ccccc1
Reaction #42016
benzoic acid
Yield 90.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)c1ccccc1
Reaction #42017
benzoic acid
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(C(=O)O)cc1
Reaction #42018
4-methylbenzoic acid
Yield 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)c1ccc(CBr)c(C(F)(F)F)c1
Reaction #42056
objective compound
Yield 60.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN1C(=O)CC[C@H]1c1cccnc1
Reaction #83823
cotinine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C(NC1=N[C@@]2(c3cc(Br)c(F)cc3F)CO[C@@H](CO)C[C@H]2CS1)c1ccccc1
Reaction #155580
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=[N+]([O-])c1ccc(CBr)c(F)c1
Reaction #586383
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
COC(=O)c1sc2cnc(S(C)=O)nc2c1-c1cccc(OC)n1
Reaction #605972
methyl 7-(6-methoxypyridin-2-yl)-2-(methylsulfinyl)thieno[3,2-d]pyrimidine-6-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
CCOC(=O)C(Br)c1ccccc1C(F)(F)F
Reaction #801837
title compound
Yield 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
COC(=O)C1CCCC(=O)C1
Reaction #802692
methyl 3-oxocyclohexanecarboxylate
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
CC(C)(c1ccc(O)cc1)c1ccc(O)cc1
Reaction #927589
bisphenol-A
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_04
CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C2=C(C)C(=O)[C@@H](O)CC2(C)C)C(C)(C)C[C@H](O)C1=O
Reaction #929531
astaxanthin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_04
CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C2=C(C)C(=O)[C@@H](O)CC2(C)C)C(C)(C)C[C@H](O)C1=O
Reaction #930544
astaxanthin
Yield 28.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_04
C=CC(=O)OCC[N+](C)(C)C.C=CC(N)=O.[Cl-]
Reaction #1050777
Acryloyloxyethyltrimethylammonium Chloride Acrylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_06
C=CC(=O)OCC[N+](C)(C)C.C=CC(N)=O.[Cl-]
Reaction #1050782
Acryloyloxyethyltrimethylammonium-Chloride Acrylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_06
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